Transport of Prions in the Peripheral Nervous System: Pathways, Cell Types, and Mechanisms

Prion diseases are transmissible protein misfolding disorders that occur in animals and humans where the endogenous prion protein, PrP(C), undergoes a conformational change into self-templating aggregates termed PrP(Sc). Formation of PrP(Sc) in the central nervous system (CNS) leads to gliosis, spon...

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Detalles Bibliográficos
Autores principales: Koshy, Sam M., Kincaid, Anthony E., Bartz, Jason C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8954800/
https://www.ncbi.nlm.nih.gov/pubmed/35337037
http://dx.doi.org/10.3390/v14030630

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8954800/
https://www.ncbi.nlm.nih.gov/pubmed/35337037
http://dx.doi.org/10.3390/v14030630

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